On December 1, 2020, the ex-Pfizer head of respiratory research Dr. Michael Yeadon and the lung specialist and former head of the public health department Dr. Wolfgang Wodarg filed an application with the EMA, the European Medicine Agency responsible for EU-wide drug approval, for the immediate suspension of all SARS CoV 2 vaccine studies, in particular the BioNtech/Pfizer study on BNT162b (EudraCT number 2020-002641-42).
Dr. Wodarg and Dr. Yeadon demand that the studies – for the protection of the life and health of the volunteers – should not be continued until a study design is available that is suitable to address the significant safety concerns expressed by an increasing number of renowned scientists against the vaccine and the study design.
On the one hand, the petitioners demand that, due to the known lack of accuracy of the PCR test in a serious study, a so-called Sanger sequencing must be used. This is the only way to make reliable statements on the effectiveness of a vaccine against Covid-19. On the basis of the many different PCR tests of highly varying quality, neither the risk of disease nor a possible vaccine benefit can be determined with the necessary certainty, which is why testing the vaccine on humans is unethical per se.
・The formation of so-called “non-neutralizing antibodies” can lead to an exaggerated immune reaction, especially when the test person is confronted with the real, “wild” virus after vaccination. This so-called antibody-dependent amplification, ADE, has long been known from experiments with corona vaccines in cats, for example. In the course of these studies all cats that initially tolerated the vaccination well died after catching the wild virus.
・The vaccinations are expected to produce antibodies against spike proteins of SARS-CoV-2. However, spike proteins also contain syncytin-homologous proteins, which are essential for the formation of the placenta in mammals such as humans. It must be absolutely ruled out that a vaccine against SARS-CoV-2 could trigger an immune reaction against syncytin-1, as otherwise infertility of indefinite duration could result in vaccinated women.
・The mRNA vaccines from BioNTech/Pfizer contain polyethylene glycol (PEG). 70% of people develop antibodies against this substance – this means that many people can develop allergic, potentially fatal reactions to the vaccination.
・The much too short duration of the study does not allow a realistic estimation of the late effects. As in the narcolepsy cases after the swine flu vaccination, millions of healthy people would be exposed to an unacceptable risk if an emergency approval were to be granted and the possibility of observing the late effects of the vaccination were to follow. Nevertheless, BioNTech/Pfizer apparently submitted an application for emergency approval on December 1, 2020.
Dr. Michael Yeadon, the former vice president and scientific director for Pfizer, has come forward with evidence that widespread SCIENCE FRAUD was used in the 2020 race for a coronavirus vaccine. In pursuit of speedy regulatory approval, Pfizer abandoned all scientific integrity. The study design for new mRNA injections is based on fraudulent diagnostic protocols that manipulate data endpoints and conceal the short and long-term adverse events inflicted by their vaccines. Dr. Yeadon is joined by German lung specialist, Dr. Wolfgang Wodarg. The two brave doctors have filed an urgent application with the European Medicine Agency, calling out the BioNtech/Pfizer vaccine study because it’s based on FRAUD.
ファイザーの元副社長兼科学ディレクターであるマイケル・イェードン博士は、2020年のコロナウイルスワクチンの競争において、広範な『科学的不正行為』が使用されたという証拠を持って名乗り出ました。迅速な規制当局の承認を目指して、ファイザーはすべての科学的整合性を放棄しました。新しいmRNA注射のための研究計画は、データのエンドポイント(評価項目)を操作し彼らのワクチンによって引き起こされる短期および長期の有害事象を隠す詐欺的な診断プロトコルに基づいています。Yeadon博士はドイツの肺の専門家であるWolfgang Wodarg博士と一緒に活動しています。二人の勇敢な医師は、BioNtech/Pfizerのワクチン研究は『不正』に基づいているとして、欧州医学庁に緊急申請を提出しました。 0097名無しさん@お腹いっぱい。2021/01/24(日) 03:42:38.71ID:4vt5eTA4https://www.distributednews.com/481367.html Pfizer's vaccine studies are based on FRAUD and put lives in danger, warns former Pfizer vice president
■mRNA vaccine studies are based on fraud, conceal serious vaccine injuries
■mRNAワクチンの研究は不正に基づいており、深刻なワクチンの被害を隠す
The doctors concur that Pfizer’s vaccine studies should be halted until a credible study design can be presented, one that doesn’t falsify data endpoints and one that addresses a host of serious safety concerns. The doctors warn that Pfizer is conflating non-specific symptoms of illness with COVID-19 diagnoses for the control arm while using inaccurate, high cycle PCR tests for a diagnosis. The doctors warn that the vaccine’s efficacy is being contorted because the study design fails to properly diagnose cases of COVID-19 and fails to confirm infection using the Sanger sequencing method. They conclude that risk of disease and potential vaccine benefit cannot be measured or determined with accuracy. They demand a halt to all human experimentation with these mRNA injections. Wodarg and Yeadon also warn that the vaccine’s efficacy toward spike proteins of SARS-CoV-2 is a real measurement of immune reaction, but this effect will also cause autoimmune issues as well.
Among these autoimmune issues is the destruction of the female reproductive system. The vaccines will produce temporary antibodies to coronavirus by attacking the spike’s syncytin-homologous proteins. Not coincidentally, the syncytin-1 is also essential for the formation of the placenta in mammals and humans. Therefore, the vaccines could cause infertility, miscarriage and birth defects, and Pfizer is not disclosing this information to patients. The use of polyethylene glycol will also cause autoimmune reactions, a problem already being observed in U.K. patients. A 2016 study in Analytical Chemistry found anti-PEG antibodies in 72 percent of human samples, and 8 percent of those samples contained high levels, which led to increased adverse events and waning vaccine efficacy.
これらの自己免疫問題の中には、女性の生殖器系の破壊があります。ワクチンは、スパイクのシンシチン同族体蛋白質を攻撃することで、コロナウイルスに対する一時的な抗体を産生します。偶然ではありませんが、シンシチン-1は哺乳類やヒトの胎盤形成にも欠かせません。そのため、ワクチンは不妊や流産、先天異常を引き起こす可能性がありますが、ファイザー社は患者にこの情報を開示していません。ポリエチレングリコールの使用もまた自己免疫反応を引き起こす可能性があり、英国の患者ではすでに問題となっています。2016年の『Analytical Chemistry』誌の研究では、有害事象が増加しワクチンの有効性が薄れてしまう抗PEG抗体がヒトサンプルの72%に検出され、そのうちの8%に高濃度の抗体が含まれていました。 0098名無しさん@お腹いっぱい。2021/01/24(日) 03:44:09.98ID:4vt5eTA4https://www.distributednews.com/481367.html Pfizer's vaccine studies are based on FRAUD and put lives in danger, warns former Pfizer vice president
Even more concerning is the vaccine’s potential for pathogenic priming. The doctors warn that the vaccine can cause the formation of so-called “non-neutralizing antibodies" that caused death to animals in prior coronavirus studies. Because the vaccine is not tested for its real-life preventative effect when humans are re-introduced to the wild virus, any claims of effectiveness are FRAUD. There’s no evidence that the vaccine actually prevents infection. In fact, the opposite evidence is true. All animal studies for coronavirus vaccines show an influx of non-neutralizing antibodies that causes an exaggerated immune response. When the animal is exposed to the wild virus later, their immune system overreacts, destroying itself. This overactive immune response caused the death of all the animals exploited in the study. These animal studies were bypassed for the COVID-19 vaccine trials because the scientists were well aware of animal fatalities from previous coronavirus experiments. This antibody-dependent amplification occurs after vaccination, but the damage is concealed until weeks or months later, when the animal or person is exposed to the wild virus in real-time. This deadly immune reaction is caused by the vaccine, but will ultimately be blamed on the subsequent wild virus infection. This is the perfect alibi for criminal vaccine makers like Pfizer.